, and delivers complete, high quality and reliable clinical trial data in a timely manner for assigned projects Responsible for end... and standardization Chairs Data Quality Review meetings with cross functional study team members to ensure on-going review of trial data...
regulatory landscape, assessing regulatory risk, and developing global filing strategies. Co-lead marketing application... more: . Position Summary The Associate Director, GRS PMDH leads global regulatory strategies to support the development and approval...
to trial design, protocol development, analysis planning, interpretation of results, and preparation of regulatory submissions.... These individuals develop collaborative relationships and work effectively with the Biostatistics Lead, and other cross...
comprehensive programming expertise to clinical project teams to lead statistical programming teams and support the development... develop collaborative relationships and work effectively within Global Biometrics & Data Sciences (GBDS), with external...
specific research related protocol and lead others in strict adherence to the policies. Qualifications : Must have an M....D., specialization in dermatology and current medical licensure; Board certification; Prior clinical trial research experience...
, and reviewing and editing of medical documents; Follow specific research related protocol and lead others in strict adherence... certification; Prior clinical trial research experience preferred; and Previous experience in pharmaceutical-related clinical...
specific research related protocol and lead others in strict adherence to the policies. Qualifications : Must have an M....D., specialization in psychiatry and current medical licensure; Board certification; Prior clinical trial research experience preferred...
information, and reviewing and editing of medical documents; Follow specific research related protocol and lead others in strict...; Board certification; Prior clinical trial research experience preferred; and Previous experience in pharmaceutical-related...
specific research related protocol and lead others in strict adherence to the policies. Qualifications Must have an M....D., specialization in dermatology and current medical licensure; Board certification; Prior clinical trial research experience...
specific research related protocol and lead others in strict adherence to the policies. Qualifications Must have an M....D., specialization in psychiatry and current medical licensure; Board certification; Prior clinical trial research experience preferred...
specific research related protocol and lead others in strict adherence to the policies. Qualifications : Must have an M....D., specialization in psychiatry and current medical licensure; Board certification; Prior clinical trial research experience preferred...
specific research related protocol and lead others in strict adherence to the policies. Qualifications Must have an M....D. with board certification and current medical licensure; Must have prior clinical trial research experience; and Previous...
specific research related protocol and lead others in strict adherence to the policies. Qualifications Must have an M....D., specialization in psychiatry and current medical licensure; Board certification; Prior clinical trial research experience preferred...
, and reviewing and editing of medical documents; Follow specific research related protocol and lead others in strict adherence... medical licensure; Board certification; Prior clinical trial research experience preferred; and Previous experience...
and assign open items to responsible parties Prepare audit lead sheets and pull initial data from systems (i.e. mapping, trial... location. Diebold Nixdorf is not responsible for any fees related to unsolicited resumes.** We are a global company operating...
for the overall audit status. Review the audit PBC list and assign open items to responsible parties Prepare audit lead... sheets and pull initial data from systems (i.e. mapping, trial balances, data dump as needed) and historical files Collect...
and assign open items to responsible parties Prepare audit lead sheets and pull initial data from systems (i.e. mapping, trial... to unsolicited resumes.** We are a global company operating in multiple locations and entities. As we are keen to find the...
Solenis is a leading global producer of specialty chemicals focused on delivering sustainable solutions for water... strategic initiatives across the business. Key Responsibilities Lead and manage VAT-related projects across multiple...
executing complex writing assignments involving a thorough understanding of clinical trial designs and interpretation... of a multiple-document projects including functioning as the lead medical writer (e.g. Lead Writer for a CTD submission dossier...